These brothers were supposed to be healthy. Their parents were supposed to be the happiest in the world. Their family was supposed to be the strongest. However, the ideal life, or rather the dream of an ideal family, fell like a house of cards. Step by step. At first, Ivan and Mykyta were born. They are premature. On the third day of life, Ivan stops breathing. He gets into resuscitation. The next day, due to severe jaundice and pneumonia, Mykyta is also taken to the intensive care unit. Doctors say that boys cannot survive…
PROJECTS (10 of 521)
With your help Vika was provided with special food for 2 years. She is stronger and already studying in the second grade (teachers come to her home). But... without food a girl can not lose weight. She has a very dangerous disease – spinal muscular amyotrophy. She cannot walk, cannot sit without support, cannot lift the arms of gravity and generally cannot raise her hands up. All this is due to weak muscles. But her condition can be improved if you take medicine, vitamins and a complex of amino acids. Victoria also needs special food, because she is very ill gaining weight.
It's hard to imagine the feel of parents when they find out that they will have a son, how happy the father is, how they expect the birth of their first child, the time of birth is coming, a long-awaited son is born, but... it turns out that the boy has an anomaly of development of the upper sky. Doctors diagnose: Dima has chromosomal abnormalities, delayed psycho-speech development.
Already three years the philanthropists of UBB feed the whole shelter with children which did not drive to live with parents. Due to payments of philanthropists of UBB ward "Home of happy children" shelter is got monthly for delicious breakfasts, dinner, and suppers. Your contribution to 57 UAH can provide one of ward delicious and nourishing soup, porridge or thin captain. We collect a sum which will have us, to provide the feed of children of Center during June and July. Join in with kind business!
The parents of this girl hoped that a miracle would happen, and the vice in her heart would eventually disappear. However, a miracle did not happen, and 6-year-old Vika still lives with congenital defects – an open arterial duct and an open oval window. Doctors sound alarmed because they urgently need to be treated with an occluder and a spiral, and his parents should buy it themselves. However, the price of the implants is extremely large for the family.
In 2015, the life of Denys and all his family turned upside down, when the boy was diagnosed with acute lymphoblastic leukemia. Over the past two and a half years, Denis suffered a lot – bone marrow transplantation, daily procedures, administration of medications and sometimes intolerable pain, isolation from friends, relatives. Not every adult can even imagine it! On August 12, 2016, Denis came through BMT in Turkey, and the results were good at first. However, six months later, aggravation began – the necrosis of the bones and tissues of the lower leg developed and he stopped walking. Then, necrosis developed in the hip joints.
Denys was born healthy. There was no limit to the parents’ joy – they finally waited for their lovely cute baby. But the cloudless childhood of Denys did not last long. Planned BCG vaccination was done to him despite the fact that the baby at that moment was sick with rubella. The result was terrible complications that turned future of the boy and his family upside down. Now he could have finished junior school, could play football with other boys in the yard. But Denys cannot sit, walk, speak, he silently lies, and 6-7 times a day his body is shaken by epilepsy seizures.
Half year ago, Mykyta's parents stopped hoping that, perhaps, suddenly their son would get up and walk himself. Six months ago, his parents decided to act gradually and clearly plan what exactly Mykyta needs from the next rehabilitation. Six months ago, they know that in China there is a unique method of treating such children as Mykyta. Then they decided to fly to the Middle Kingdom and find out whether miracles really work there.
Illia is a 14-year-old teenager from Mariupil, who most dreams of becoming healthy, like most of his peer friends. The boy is a coveted child, he was born absolutely healthy, but at 6 months he began to have problems with the tummy: constant frustration and underweight, and from 10 months of frequent bronchitis and pneumonia, which were seriously treated. The child was examined for tuberculosis and other lung diseases, but the correct diagnosis was made only in 4 years. It is cystic fibrosis, a genetic disease that affects the pancreas and destroys the lungs.
Anna Kaplun is the director of development in the company for the production of visual advertising. "In the charity marathon I will participate for the first time. But I remember very well the experience of participating in the half-marathon, when I was running, while still nursing mom, not fully recovered after childbirth. This experience of overcoming was very important for me. I want with my help one child to take a height that seemed unattainable. I run to Sonechka Dyryavka to hear and overcome all the barriers in communication.